Biostatistician - Bilingual Mandarin

Systimmune; Bothell (WA); On-site; USD 80,000 - 140,000; Full time

Benefits offered by this job

Medical, dental, vision premiums paid

401(k) with company match

PTO and holidays

Job summary

SystImmune, a leading clinical-stage biopharmaceutical company, seeks a full-time Biostatistician to join our on-site team in Bothell, WA starting September 2026. You will support data cleaning, analysis, and reporting for new cancer therapies using SAS, R, or Python, collaborating with senior biostatisticians on clinical and non-clinical studies.

The role requires a Master’s or PhD in Biostatistics (or related field), plus 3+ years of statistical work experience, with Mandarin fluency and

Qualifications

• Master’s or PhD in Biostatistics or related field with 3+ years of statistical work experience.
• Fluency in Mandarin is required.
• Experience with SAS, R, or Python for data analysis.
• CDISC/CDASH standards experience.
• Strong clinical trial design and data analysis knowledge.
• Excellent written and oral communication skills.

Responsibilities

• Provide data-driven statistical support to clinical teams and guidance on data challenges.
• Collaborate on study design and protocol development.
• Develop and validate SAS programs; perform data analysis and generate tables/listings/figures.
• Interpret interim analyses and pharmacokinetics analyses for decision making.
• Prepare SAPs and review CSR/SAR deliverables.
• Oversee CRO programming and ensure SDTM/ADaM compliance.
• Quality control project deliverables and ensure data integrity.
• Perform ad-hoc analyses and simulations as needed.
• Apply regulatory guidelines and industry standards in statistics and SAS programming.

Skills

Mandarin fluency

Communication skills

Statistical concepts understanding

Clinical trial design knowledge

Education

Master’s Degree in Biostatistics

Ph.D. in Biostatistics or related field

Tools

SAS

R

Python

Job description

About the Role

SystImmune is a leading and well‑funded clinical‑stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi‑specific, multi‑specific antibodies, and antibody‑drug conjugates (ADCs). The biostatistician will collaborate with senior biostatisticians on clinical or non‑clinical studies, leveraging data science and statistics expertise to support data cleaning, visualization, analysis, and reporting for new drug discovery efforts. The position requires full‑time onsite presence at our Bothell, WA office starting September 2026.

Responsibilities

• Provide data‑driven insights and statistical support to clinical teams, offering guidance on data‑related challenges and participating in project team meetings as needed.
• Collaborate with clinical teams on study design and clinical study protocol development.
• Develop, validate, and maintain programs (e.g., SAS program) and conduct comprehensive data analysis using SAS, R, or other statistical software to generate TLFs as needed.
• Conduct and interpret interim analysis, including statistical and pharmacokinetics analysis, to support clinical decision making.
• Develop and review SAP, including table/listing/figure shells, and review final SAR and CSR.
• Oversee and validate CRO programming activities, ensuring accuracy in internally or externally produced SDTM, ADaM, SAS tables, listings, and figures.
• Conduct quality control of project deliverables, ensuring compliance with data integrity and reporting standards.
• Perform simulations and ad‑hoc statistical analysis when needed.
• Understand and apply regulatory guidelines and industry standard practices on statistics and SAS programming.

Qualifications

• Master’s Degree with 3+ years of statistical work experience or Ph.D. in Biostatistics, Statistics, or related field.
• Fluency in Mandarin.
• Experience with statistical programming such as SAS, R, or Python.
• Experience with CDISC and CDASH standards.
• Strong knowledge and experience in clinical trial design and data analysis, with ability to communicate statistical concepts.
• Strong knowledge of applied statistics and data analysis methodology including regression modeling, categorical data analysis, survival analysis, etc.
• Strong knowledge of clinical research, drug development process, and medical terminology; oncology experience preferred.
• Excellent oral and written communication skills.
• Excellent presentation skills.

Salary & Benefits

Expected base salary range is $80,000 – $140,000 annually. Compensation decisions will be based on qualifications, experience, and skills, with most offers falling in the low to mid‑point of the range but potentially extending toward the higher end for exceptional candidates. Benefits include 100% paid employee premiums for medical, dental, and vision, STD, LTD, a 401(k) plan with a 50% company match up to 3% with a 5‑year vesting schedule, 15 PTO days per year, sick leave, and 11 paid holidays.

Equal Opportunity

SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.